Linked Data
ClinVar Variation Id:
1970670
ClinVar RCV Id:
RCV002760461
dbSNP Id:
rs2058814393
gnomAD v4:
3-12600144-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12600144A>G , CM000665.2:g.12600144A>G | GRCh38 |
| NC_000003.11:g.12641643A>G , CM000665.1:g.12641643A>G | GRCh37 |
| NC_000003.10:g.12616643A>G | NCBI36 |
| NG_007467.1:g.69036T>C , LRG_413:g.69036T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*655+8T>C | ENSP00000401088.1:n.*655+8T>C | |
| ENST00000432427.3:c.310+8T>C | ||
| ENST00000465826.6:n.581+8T>C | ||
| ENST00000491290.2:n.1367+8T>C | ||
| ENST00000684903.1:c.*667+8T>C | ENSP00000508612.1:n.*667+8T>C | |
| ENST00000685348.1:c.*667+8T>C | ENSP00000510285.1:n.*667+8T>C | |
| ENST00000685437.1:c.891+8T>C | ENSP00000508794.1:n.891+8T>C | |
| ENST00000685653.1:c.990+8T>C | ENSP00000509968.1:n.990+8T>C | |
| ENST00000685738.1:c.990+8T>C | ENSP00000510156.1:n.990+8T>C | |
| ENST00000686409.1:n.1706T>C | ||
| ENST00000686455.1:n.1353+8T>C | ||
| ENST00000686479.1:n.1361+8T>C | ||
| ENST00000686762.1:c.990+8T>C | ENSP00000509767.1:n.990+8T>C | |
| ENST00000687257.1:n.1226+8T>C | ||
| ENST00000687326.1:c.990+8T>C | ENSP00000509665.1:n.990+8T>C | |
| ENST00000687486.1:c.182+244T>C | ||
| ENST00000687505.1:n.1108+8T>C | ||
| ENST00000687923.1:c.891+8T>C | ENSP00000510255.1:n.891+8T>C | |
| ENST00000687940.1:n.1367+8T>C | ||
| ENST00000688269.1:n.1586+8T>C | ||
| ENST00000688326.1:c.310+8T>C | ||
| ENST00000688444.1:n.1316+8T>C | ||
| ENST00000688543.1:c.891+8T>C | ENSP00000509612.1:n.891+8T>C | |
| ENST00000688625.1:c.*568+8T>C | ENSP00000509522.1:n.*568+8T>C | |
| ENST00000688803.1:n.1221+8T>C | ||
| ENST00000689097.1:c.*667+8T>C | ENSP00000509756.1:n.*667+8T>C | |
| ENST00000689389.1:c.990+8T>C | ENSP00000510213.1:n.990+8T>C | |
| ENST00000689418.1:c.*667+8T>C | ENSP00000509467.1:n.*667+8T>C | |
| ENST00000689481.1:c.*667+8T>C | ENSP00000510248.1:n.*667+8T>C | |
| ENST00000689540.1:n.1140+8T>C | ||
| ENST00000689876.1:c.990+8T>C | ENSP00000508535.1:n.990+8T>C | |
| ENST00000689914.1:c.990+8T>C | ENSP00000509847.1:n.990+8T>C | |
| ENST00000690397.1:c.879+8T>C | ENSP00000508730.1:n.879+8T>C | |
| ENST00000690460.1:c.978+8T>C | ENSP00000509106.1:n.978+8T>C | |
| ENST00000690625.1:n.1293+8T>C | ||
| ENST00000691268.1:c.417+8T>C | ||
| ENST00000691396.1:c.*783+8T>C | ENSP00000510712.1:n.*783+8T>C | |
| ENST00000691724.1:c.990+8T>C | ENSP00000509255.1:n.990+8T>C | |
| ENST00000691779.1:c.*568+8T>C | ENSP00000508592.1:n.*568+8T>C | |
| ENST00000691899.1:c.990+8T>C | ENSP00000508763.1:n.990+8T>C | |
| ENST00000692069.1:n.1221T>C | ||
| ENST00000692093.1:c.891+8T>C | ENSP00000509669.1:n.891+8T>C | |
| ENST00000692311.1:n.1479T>C | ||
| ENST00000692558.1:n.1355+8T>C | ||
| ENST00000692773.1:c.*727+8T>C | ENSP00000509055.1:n.*727+8T>C | |
| ENST00000692830.1:c.*735+8T>C | ENSP00000509461.1:n.*735+8T>C | |
| ENST00000693069.1:c.891+8T>C | ENSP00000510072.1:n.891+8T>C | |
| ENST00000693312.1:c.765+8T>C | ENSP00000508686.1:n.765+8T>C | |
| ENST00000693664.1:c.990+8T>C | ENSP00000509614.1:n.990+8T>C | |
| ENST00000693705.1:c.*667+8T>C | ENSP00000510697.1:n.*667+8T>C | |
| ENST00000251849.9:c.990+8T>C MANE Select | ENSP00000251849.4:n.990+8T>C | |
| ENST00000442415.7:c.1050+8T>C | ENSP00000401888.2:n.1050+8T>C | |
| ENST00000251849.8:c.990+8T>C | ENSP00000251849.4:n.990+8T>C | |
| ENST00000423275.5:c.*667+8T>C | ENSP00000401088.1:n.*667+8T>C | |
| ENST00000432427.2:c.627+8T>C | ENSP00000398591.2:n.627+8T>C | |
| ENST00000442415.6:c.1050+8T>C | ENSP00000401888.2:n.1050+8T>C | |
| ENST00000465826.5:n.234+8T>C | ||
| NM_002880.3:c.990+8T>C , LRG_413t1:c.990+8T>C | NP_002871.1:n.990+8T>C | |
| XM_005265355.1:c.990+8T>C | XP_005265412.1:n.990+8T>C | |
| XM_005265357.1:c.891+8T>C | XP_005265414.1:n.891+8T>C | |
| XM_005265358.3:c.747+8T>C | XP_005265415.1:n.747+8T>C | |
| XM_005265359.3:c.648+8T>C | XP_005265416.1:n.648+8T>C | |
| XM_005265360.1:c.990+8T>C | XP_005265417.1:n.990+8T>C | |
| XM_011533974.1:c.990+8T>C | XP_011532276.1:n.990+8T>C | |
| XM_011533975.1:c.747+8T>C | XP_011532277.1:n.747+8T>C | |
| NM_001354689.1:c.1050+8T>C | NP_001341618.1:n.1050+8T>C | |
| NM_001354690.1:c.990+8T>C | NP_001341619.1:n.990+8T>C | |
| NM_001354691.1:c.747+8T>C | NP_001341620.1:n.747+8T>C | |
| NM_001354692.1:c.747+8T>C | NP_001341621.1:n.747+8T>C | |
| NM_001354693.1:c.891+8T>C | NP_001341622.1:n.891+8T>C | |
| NM_001354694.1:c.807+8T>C | NP_001341623.1:n.807+8T>C | |
| NM_001354695.1:c.648+8T>C | NP_001341624.1:n.648+8T>C | |
| NR_148940.1:n.1405+8T>C | ||
| NR_148941.1:n.1405+8T>C | ||
| NR_148942.1:n.1405+8T>C | ||
| XM_011533974.3:c.990+8T>C | XP_011532276.1:n.990+8T>C | |
| XM_017006966.1:c.891+8T>C | XP_016862455.1:n.891+8T>C | |
| XR_001740227.1:n.1222+8T>C | ||
| NM_001354689.3:c.1050+8T>C | NP_001341618.1:n.1050+8T>C | |
| NM_001354690.2:c.990+8T>C | NP_001341619.1:n.990+8T>C | |
| NM_001354691.2:c.747+8T>C | NP_001341620.1:n.747+8T>C | |
| NM_001354692.2:c.747+8T>C | NP_001341621.1:n.747+8T>C | |
| NM_001354693.2:c.891+8T>C | NP_001341622.1:n.891+8T>C | |
| NM_001354694.2:c.807+8T>C | NP_001341623.1:n.807+8T>C | |
| NM_001354695.2:c.648+8T>C | NP_001341624.1:n.648+8T>C | |
| NR_148940.2:n.1321+8T>C | ||
| NR_148941.2:n.1321+8T>C | ||
| NR_148942.2:n.1321+8T>C | ||
| NM_001354690.3:c.990+8T>C | NP_001341619.1:n.990+8T>C | |
| NM_001354691.3:c.747+8T>C | NP_001341620.1:n.747+8T>C | |
| NM_001354692.3:c.747+8T>C | NP_001341621.1:n.747+8T>C | |
| NM_001354693.3:c.891+8T>C | NP_001341622.1:n.891+8T>C | |
| NM_001354694.3:c.807+8T>C | NP_001341623.1:n.807+8T>C | |
| NM_001354695.3:c.648+8T>C | NP_001341624.1:n.648+8T>C | |
| NM_002880.4:c.990+8T>C MANE Select | NP_002871.1:n.990+8T>C | |
| NR_148940.3:n.1321+8T>C | ||
| NR_148941.3:n.1321+8T>C | ||
| NR_148942.3:n.1321+8T>C |